Green Pea - 49288-0380-4 - (Green Pea)

Alphabetical Index


Drug Information of Green Pea

Product NDC: 49288-0380
Proprietary Name: Green Pea
Non Proprietary Name: Green Pea
Active Ingredient(s): .05    g/mL & nbsp;   Green Pea
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Green Pea

Product NDC: 49288-0380
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Green Pea

Package NDC: 49288-0380-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0380-4)

NDC Information of Green Pea

NDC Code 49288-0380-4
Proprietary Name Green Pea
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0380-4)
Product NDC 49288-0380
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Green Pea
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name PEA
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient]

Complete Information of Green Pea


General Information